CASE REPORT
Cardiovascular Disorders http://dx.doi.org/10.3346/jkms.2014.29.9.1317 • J Korean Med Sci 2014; 29: 1317-1319
Extremely Elevated International Normalized Ratio of Warfarin in a Patient with CYP2C9*1/*3 and Thyrotoxicosis Ji Eun Lee,1 Duck Hyun Ryu,1 Ho Jung Jeong,1 Jung Hoon Kim,1 Ji Eun Jun,1 June Soo Kim,1 and Soo Youn Lee2 Departments of 1Medicine, and 2Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea Received: 7 December 2013 Accepted: 26 May 2014
A 73-yr-old Korean man with permanent atrial fibrillation visited outpatient clinic with severely increased International Normalized Ratio (INR) values after taking a usual starting dosage of warfarin to prevent thromboembolism. We found out later from his blood tests that he had hyperthyroidism at the time of treatment initiation. His genetic analysis showed CYP2C9*1/*3 and VKORC1+1173TT genotypes. We suspect that both hyperthyroidism and genetic variant would have contributed to his extremely increased INR at the beginning of warfarin therapy. From this case, we learned that pharmacogenetic and thyroid function test might be useful when deciding the starting dosage of warfarin in patients with atrial fibrillation. Keywords: Warfarin; International Normalized Ratio; Thyrotoxicosis; Genotype
Address for Correspondence: June Soo Kim, MD Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 135-710, Korea Tel: +82.2-3410-3414, Fax: +82.2-3410-3849 E-mail: [email protected]
INTRODUCTION
CASE DESCRIPTION
Warfarin is the most widely used anticoagulant agent for the prevention of stroke or systemic thromboembolism in patients with atrial fibrillation. However, warfarin has a narrow therapeutic range of international normalized ratio (INR) and is known to have multiple interactions with drugs, food, and herb. There is some difficulty in deciding a starting dosage of warfarin, because of the large interindividual variation in the dose needed to reach adequate level of INR. The warfarin dose can be affected by several factors including dietary, demographic factors, drugs and, several pathophysiological conditions (1). Genetic factors also play a relevant role in the individual variability of the warfarin dose. In particular, several single nucleotide polymorphisms of the cytochrome P450 (CYP), subfamily IIC, polypeptide 9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genes can significantly influence the warfarin dose requirement (2). Clinical factors, such as thyrotoxicosis, can either strengthen or reduce warfarin action. Several coagulation and fibrinolytic parameters appear to be affected by thyroid hormone excess (3). We report a patient with atrial fibrillation in whom the concomitant presence of rare genetic abnormality and thyrotoxicosis caused a marked increase in the INR level at the beginning of warfarin therapy.
A 73-yr-old Korean male with permanent atrial fibrillation visited outpatient clinic for the management of atrial fibrillation on Feb. 21, 2012. He had a history of hypertension and colon cancer with liver metastasis. At the age of 68, he had undergone extended right hemicolectomy with liver tumorectomy due to colon cancer with liver metastasis and received adjuvant chemotherapy for two years. After chemotherapy, he had no evidence of tumor recurrence. His current medication included diltiazem (90 mg/day) and aspirin (100 mg/day), spironolactone (25 mg/day), hydrochlorothiazide (12.5 mg/day). Considering his risk for stroke and systemic thromboembolism (CHA2DS2-VASc score 2), oral anticoagulation was recommended for him. He began to take warfarin 3 mg daily since March 6, 2012. When he revisited the outpatient clinic after six days, his INR was significantly increased to 15 (Fig. 1). He had recently experienced epistaxis and melena. He was admitted for correction of high INR and bleeding tendency on March 12, 2012. His liver function test at the time of admission was normal and he had no short bowel syndrome which would affect drug absorption. He denied any drug, alcohol, or herbal intake, which may affect INR level. We also performed a pharmacogenetic test on him to identify genetic susceptibility to warfarin effect. Genomic DNA was extracted from peripheral blood leukocytes using DNA extract
© 2014 The Korean Academy of Medical Sciences. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
pISSN 1011-8934 eISSN 1598-6357
Lee JE, et al. • Elevated INR of Warfarin in Thyrotoxicosis Warfarin 3 mg 6 days
Aspirin 100 mg 15.00
15 Warfarin start 2012/03/16
10
INR
Melena epistaxis
Weight loss tremor
5
3.45
1.25
0 2012/01/14
1.53
1.68
1.68
1.45
1.85
1.42
1.36
03/12 03/13 03/14 03/15 03/16 03/17 03/18 03/19 03/20
Date Plasma warfarin 7-OH-warfarin Ratio (warfarin/7-OH-warfarin)
0.793 μg/mL 0.046 μg/mL 7.2
0.178 μg/mL 0.01 μg/mL 18
Treatment Diagnostic test Result
Vitamin K Pharmacogenetic test CYP2C9*1/*3, VKORC1 1173TT
Vitamin K Thyroid function test T3 (437.84 ng/dL), T4 (17.6 μg/dL), TSH (0.01 μIU/mL) Free T4 (6.86 ng/dL). Admission
all lysis reagents (Applied Biosystems, CA, USA). Genotyping for polymorphisms of CYP2C9 (rs1057910, CYP2C9*3) and VKORC1 (rs9934438, 1173C > T) variants was performed using TaqMan® Drug Metabolism Genotyping Assays and 7500 Fast Real-time PCR system (Applied Biosystems, CA, USA). Later, he was found to be an intermediate metabolizer with genotype of CYP2C9*1/*3 and had VKORC1+1173TT genotype indicating high warfarin sensitivity (Fig. 1). Upon admission, warfarin was discontinued and 10 mg of Vitamin K was injected 2 times. Then on hospital day (HD) 3, aspirin 100 mg a day was started to replace warfarin. But his INR was increased to 3.45 again on the same day (Fig. 1). We measured his plasma warfarin and 7-hydroxy-warfarin concentrations by high-performance liquid chromatography tandem mass spectrometry on HD 0 as a baseline and HD 3. On HD 0, total plasma warfarin, 7-hydroxy-warfarin concentration (7-OH-warfarin), and the ratio of warfarin/7-OH-warfarin were 0.793 µg/mL (therapeutic range 0.5 to 3.0 µg/mL), 0.046 µg/mL, and 7.2, respectively. On HD 3, total plasma warfarin and 7-OH-warfarin levels were decreased to 0.178 µg/mL and 0.01 µg/mL, respectively, and the ratio of warfarin/7-OH-warfarin was increased to 18 (Fig. 1). On thorough history taking, he complained of hand tremor with proximal muscle weakness. He also experienced unexplain ed body weight loss before admission. From this information, we suspected hyperthyroidism and thyroid function test was performed on HD 3 to confirm the diagnosis. Total T3, total T4, TSH, and free T4 were 437.84 ng/dL (normal range 60 to 181
1318 http://jkms.org
Fig. 1. Treatment course.
ng/dL), 17.6 µg/dL (normal range 3.2 to 12.6 µg/dL), 0.01 µIU/ mL (normal range 0.64 to 6.27 µIU/mL), and 6.86 ng/dL (normal range 0.89 to 1.8 ng/dL), respectively. The results were consistent with hyperthyroidism, so carbimazole (20 mg twice daily) and betaxolol (20 mg twice daily) were started. The patient was discharged from the hospital on HD 8. His INR was 1.36 at the time of discharge (Fig. 1). After discharge, warfarin was discontinued due to the risk of bleeding and instead aspirin was maintained for atrial fibrillation.
DISCUSSION We have observed a rare case with genotype of CYP2C9*1/*3 and concomitant hyperthyroidism in which the usual initiation of warfarin therapy caused a dangerous and unexpected elevation of the INR value and led to bleeding complication. CYP2C9 is a liver enzyme required for the oxidative metabolism of a large number of clinically important drugs, including warfarin. Three alleles, CYP2C9*1, *2, and *3 are present in most ethnic populations. Both CYP2C9*2 and *3, and only in carriers of at least 1 copy of CYP2C9*3 confer significantly higher risk for warfarin over-anticoagulation and hemorrhagic complications compared to wild type allele (4). The frequency of CYP2C9 and VKORC1 1173 C/T polymorphism is largely dependent on ethnicity. In a Korean population study, the allele frequencies of CYP2C9*3 and CYP2C9*1 are reported to be 6% and 93.4%, respectively. But CYP2C9*2 allele has not been detected. The frequencies of CYP2C9 *1/*3* and http://dx.doi.org/10.3346/jkms.2014.29.9.1317
Lee JE, et al. • Elevated INR of Warfarin in Thyrotoxicosis 1/*1 genotypes are 12% and 86.9%, respectively (5). VKORC1+ 1173TT genotype associated with high warfarin sensitivity predominates in Asian population than in non-Asian population (6). It has been reported that overt hyperthyroidism exerts a procoagulant effect and increases the risk of thromboembolic events (5). In contrast, thyrotoxicosis has been associated with an increased sensitivity to warfarin, irrespective of the nature of the underlying thyroid disease (6). Several studies reported warfarin-induced hypoprothrombinemia in hyperthyroidism with an increased risk of bleeding (7-10). In thyrotoxic patients, warfarin produced a greater fall in factors (II and VII) and a greater increase in prothrombin time than in the euthyroid state (11). Furthermore in thyrotoxicosis, the degradation rate of coagulation factors is increased, resulting in their higher plasma clearance and shorter plasma half-life (6). We are presenting a very rare case about a patient with an uncommon genetic susceptibility to warfarin effect and co-existing hyperthyroidism at the beginning of warfarin treatment. From this case, we learned the clinical usefulness of pharmacogenetic and thyroid function tests in patients with atrial fibrillation, in whom warfarin is considered to prevent stroke or systemic thromboembolism.
ORCID
REFERENCES 1. Eriksson N, Wadelius M. Prediction of warfarin dose: why, when and how? Pharmacogenomics 2012; 13: 429-40. 2. Klein TE, Altman RB, Eriksson N, Gage BF, Kimmel SE, Lee MT, Limdi NA, Page D, Roden DM, Wagner MJ, et al. Estimation of the warfarin dose with clinical and pharmacogenetic data. N Engl J Med 2009; 360: 753-64. 3. Stuijver DJ, van Zaane B, Romualdi E, Brandjes DP, Gerdes VE, Squizzato A. The effect of hyperthyroidism on procoagulant, anticoagulant and fibrinolytic factors: a systematic review and meta-analysis. Thromb Haemost 2012; 108: 1077-88. 4. Ma C, Zhang Y, Xu Q, Yang J, Zhang Y, Gao L, Xu B, Wang H, Li Y, Lu C, et al. Influence of warfarin dose-associated genotypes on the risk of hemorrhagic complications in Chinese patients on warfarin. Int J Hematol 2012; 96: 719-28. 5. Squizzato A, Romualdi E, Büller HR, Gerdes VE. Clinical review: thyroid dysfunction and effects on coagulation and fibrinolysis: a systematic review. J Clin Endocrinol Metab 2007; 92: 2415-20. 6. Kurnik D, Loebstein R, Farfel Z, Ezra D, Halkin H, Olchovsky D. Complex drug-drug-disease interactions between amiodarone, warfarin, and the thyroid gland. Medicine (Baltimore) 2004; 83: 107-13. 7. Self T, Weisburst M, Wooten E, Straughn A, Oliver J. Warfarin-induced hypoprothrombinemia. Potentiation by hyperthyroidism. JAMA 1975; 231: 1165-6. 8. Vagenakis AG, Cote R, Miller ME, Braverman LE, Stohlman F Jr. Enhancement of warfarin-induced hypoprothrombinemia by thyrotoxicosis. Johns Hopkins Med J 1972; 131: 69-73.
Ji Eun Lee http://orcid.org/0000-0002-8660-0861 Duck Hyun Ryu http://orcid.org/0000-0003-1426-8318 Ho Jung Jeong http://orcid.org/0000-0003-2944-2294 Jung Hoon Kim http://orcid.org/0000-0003-3140-1328 Ji Eun Jun http://orcid.org/0000-0002-7204-4913 June Soo Kim http://orcid.org/0000-0001-7569-6450 Soo Youn Lee http://orcid.org/0000-0002-0662-7408
9. Olchovsky D, Pines A, Zwas ST, Itzchak Y, Halkin H. Apathetic thyrotoxicosis due to hemorrhage into a hyperfunctioning thyroid nodule after excessive anticoagulation. South Med J 1985; 78: 609-11. 10. Tomisti L, Del Re M, Bartalena L, Tanda ML, Pucci A, Pambianco F, Da nesi R, Braverman LE, Martino E, Bogazzi F. Effects of amiodarone, thyroid hormones and CYP2C9 and VKORC1 polymorphisms on warfarin metabolism: a review of the literature. Endocr Pract 2013; 19: 1043-9. 11. Kellett HA, Sawers JS, Boulton FE, Cholerton S, Park BK, Toft AD. Problems of anticoagulation with warfarin in hyperthyroidism. Q J Med 1986; 58: 43-51.
http://dx.doi.org/10.3346/jkms.2014.29.9.1317
http://jkms.org 1319
Cardiovascular Disorders http://dx.doi.org/10.3346/jkms.2014.29.9.1317 • J Korean Med Sci 2014; 29: 1317-1319
Extremely Elevated International Normalized Ratio of Warfarin in a Patient with CYP2C9*1/*3 and Thyrotoxicosis Ji Eun Lee,1 Duck Hyun Ryu,1 Ho Jung Jeong,1 Jung Hoon Kim,1 Ji Eun Jun,1 June Soo Kim,1 and Soo Youn Lee2 Departments of 1Medicine, and 2Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea Received: 7 December 2013 Accepted: 26 May 2014
A 73-yr-old Korean man with permanent atrial fibrillation visited outpatient clinic with severely increased International Normalized Ratio (INR) values after taking a usual starting dosage of warfarin to prevent thromboembolism. We found out later from his blood tests that he had hyperthyroidism at the time of treatment initiation. His genetic analysis showed CYP2C9*1/*3 and VKORC1+1173TT genotypes. We suspect that both hyperthyroidism and genetic variant would have contributed to his extremely increased INR at the beginning of warfarin therapy. From this case, we learned that pharmacogenetic and thyroid function test might be useful when deciding the starting dosage of warfarin in patients with atrial fibrillation. Keywords: Warfarin; International Normalized Ratio; Thyrotoxicosis; Genotype
Address for Correspondence: June Soo Kim, MD Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 135-710, Korea Tel: +82.2-3410-3414, Fax: +82.2-3410-3849 E-mail: [email protected]
INTRODUCTION
CASE DESCRIPTION
Warfarin is the most widely used anticoagulant agent for the prevention of stroke or systemic thromboembolism in patients with atrial fibrillation. However, warfarin has a narrow therapeutic range of international normalized ratio (INR) and is known to have multiple interactions with drugs, food, and herb. There is some difficulty in deciding a starting dosage of warfarin, because of the large interindividual variation in the dose needed to reach adequate level of INR. The warfarin dose can be affected by several factors including dietary, demographic factors, drugs and, several pathophysiological conditions (1). Genetic factors also play a relevant role in the individual variability of the warfarin dose. In particular, several single nucleotide polymorphisms of the cytochrome P450 (CYP), subfamily IIC, polypeptide 9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genes can significantly influence the warfarin dose requirement (2). Clinical factors, such as thyrotoxicosis, can either strengthen or reduce warfarin action. Several coagulation and fibrinolytic parameters appear to be affected by thyroid hormone excess (3). We report a patient with atrial fibrillation in whom the concomitant presence of rare genetic abnormality and thyrotoxicosis caused a marked increase in the INR level at the beginning of warfarin therapy.
A 73-yr-old Korean male with permanent atrial fibrillation visited outpatient clinic for the management of atrial fibrillation on Feb. 21, 2012. He had a history of hypertension and colon cancer with liver metastasis. At the age of 68, he had undergone extended right hemicolectomy with liver tumorectomy due to colon cancer with liver metastasis and received adjuvant chemotherapy for two years. After chemotherapy, he had no evidence of tumor recurrence. His current medication included diltiazem (90 mg/day) and aspirin (100 mg/day), spironolactone (25 mg/day), hydrochlorothiazide (12.5 mg/day). Considering his risk for stroke and systemic thromboembolism (CHA2DS2-VASc score 2), oral anticoagulation was recommended for him. He began to take warfarin 3 mg daily since March 6, 2012. When he revisited the outpatient clinic after six days, his INR was significantly increased to 15 (Fig. 1). He had recently experienced epistaxis and melena. He was admitted for correction of high INR and bleeding tendency on March 12, 2012. His liver function test at the time of admission was normal and he had no short bowel syndrome which would affect drug absorption. He denied any drug, alcohol, or herbal intake, which may affect INR level. We also performed a pharmacogenetic test on him to identify genetic susceptibility to warfarin effect. Genomic DNA was extracted from peripheral blood leukocytes using DNA extract
© 2014 The Korean Academy of Medical Sciences. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
pISSN 1011-8934 eISSN 1598-6357
Lee JE, et al. • Elevated INR of Warfarin in Thyrotoxicosis Warfarin 3 mg 6 days
Aspirin 100 mg 15.00
15 Warfarin start 2012/03/16
10
INR
Melena epistaxis
Weight loss tremor
5
3.45
1.25
0 2012/01/14
1.53
1.68
1.68
1.45
1.85
1.42
1.36
03/12 03/13 03/14 03/15 03/16 03/17 03/18 03/19 03/20
Date Plasma warfarin 7-OH-warfarin Ratio (warfarin/7-OH-warfarin)
0.793 μg/mL 0.046 μg/mL 7.2
0.178 μg/mL 0.01 μg/mL 18
Treatment Diagnostic test Result
Vitamin K Pharmacogenetic test CYP2C9*1/*3, VKORC1 1173TT
Vitamin K Thyroid function test T3 (437.84 ng/dL), T4 (17.6 μg/dL), TSH (0.01 μIU/mL) Free T4 (6.86 ng/dL). Admission
all lysis reagents (Applied Biosystems, CA, USA). Genotyping for polymorphisms of CYP2C9 (rs1057910, CYP2C9*3) and VKORC1 (rs9934438, 1173C > T) variants was performed using TaqMan® Drug Metabolism Genotyping Assays and 7500 Fast Real-time PCR system (Applied Biosystems, CA, USA). Later, he was found to be an intermediate metabolizer with genotype of CYP2C9*1/*3 and had VKORC1+1173TT genotype indicating high warfarin sensitivity (Fig. 1). Upon admission, warfarin was discontinued and 10 mg of Vitamin K was injected 2 times. Then on hospital day (HD) 3, aspirin 100 mg a day was started to replace warfarin. But his INR was increased to 3.45 again on the same day (Fig. 1). We measured his plasma warfarin and 7-hydroxy-warfarin concentrations by high-performance liquid chromatography tandem mass spectrometry on HD 0 as a baseline and HD 3. On HD 0, total plasma warfarin, 7-hydroxy-warfarin concentration (7-OH-warfarin), and the ratio of warfarin/7-OH-warfarin were 0.793 µg/mL (therapeutic range 0.5 to 3.0 µg/mL), 0.046 µg/mL, and 7.2, respectively. On HD 3, total plasma warfarin and 7-OH-warfarin levels were decreased to 0.178 µg/mL and 0.01 µg/mL, respectively, and the ratio of warfarin/7-OH-warfarin was increased to 18 (Fig. 1). On thorough history taking, he complained of hand tremor with proximal muscle weakness. He also experienced unexplain ed body weight loss before admission. From this information, we suspected hyperthyroidism and thyroid function test was performed on HD 3 to confirm the diagnosis. Total T3, total T4, TSH, and free T4 were 437.84 ng/dL (normal range 60 to 181
1318 http://jkms.org
Fig. 1. Treatment course.
ng/dL), 17.6 µg/dL (normal range 3.2 to 12.6 µg/dL), 0.01 µIU/ mL (normal range 0.64 to 6.27 µIU/mL), and 6.86 ng/dL (normal range 0.89 to 1.8 ng/dL), respectively. The results were consistent with hyperthyroidism, so carbimazole (20 mg twice daily) and betaxolol (20 mg twice daily) were started. The patient was discharged from the hospital on HD 8. His INR was 1.36 at the time of discharge (Fig. 1). After discharge, warfarin was discontinued due to the risk of bleeding and instead aspirin was maintained for atrial fibrillation.
DISCUSSION We have observed a rare case with genotype of CYP2C9*1/*3 and concomitant hyperthyroidism in which the usual initiation of warfarin therapy caused a dangerous and unexpected elevation of the INR value and led to bleeding complication. CYP2C9 is a liver enzyme required for the oxidative metabolism of a large number of clinically important drugs, including warfarin. Three alleles, CYP2C9*1, *2, and *3 are present in most ethnic populations. Both CYP2C9*2 and *3, and only in carriers of at least 1 copy of CYP2C9*3 confer significantly higher risk for warfarin over-anticoagulation and hemorrhagic complications compared to wild type allele (4). The frequency of CYP2C9 and VKORC1 1173 C/T polymorphism is largely dependent on ethnicity. In a Korean population study, the allele frequencies of CYP2C9*3 and CYP2C9*1 are reported to be 6% and 93.4%, respectively. But CYP2C9*2 allele has not been detected. The frequencies of CYP2C9 *1/*3* and http://dx.doi.org/10.3346/jkms.2014.29.9.1317
Lee JE, et al. • Elevated INR of Warfarin in Thyrotoxicosis 1/*1 genotypes are 12% and 86.9%, respectively (5). VKORC1+ 1173TT genotype associated with high warfarin sensitivity predominates in Asian population than in non-Asian population (6). It has been reported that overt hyperthyroidism exerts a procoagulant effect and increases the risk of thromboembolic events (5). In contrast, thyrotoxicosis has been associated with an increased sensitivity to warfarin, irrespective of the nature of the underlying thyroid disease (6). Several studies reported warfarin-induced hypoprothrombinemia in hyperthyroidism with an increased risk of bleeding (7-10). In thyrotoxic patients, warfarin produced a greater fall in factors (II and VII) and a greater increase in prothrombin time than in the euthyroid state (11). Furthermore in thyrotoxicosis, the degradation rate of coagulation factors is increased, resulting in their higher plasma clearance and shorter plasma half-life (6). We are presenting a very rare case about a patient with an uncommon genetic susceptibility to warfarin effect and co-existing hyperthyroidism at the beginning of warfarin treatment. From this case, we learned the clinical usefulness of pharmacogenetic and thyroid function tests in patients with atrial fibrillation, in whom warfarin is considered to prevent stroke or systemic thromboembolism.
ORCID
REFERENCES 1. Eriksson N, Wadelius M. Prediction of warfarin dose: why, when and how? Pharmacogenomics 2012; 13: 429-40. 2. Klein TE, Altman RB, Eriksson N, Gage BF, Kimmel SE, Lee MT, Limdi NA, Page D, Roden DM, Wagner MJ, et al. Estimation of the warfarin dose with clinical and pharmacogenetic data. N Engl J Med 2009; 360: 753-64. 3. Stuijver DJ, van Zaane B, Romualdi E, Brandjes DP, Gerdes VE, Squizzato A. The effect of hyperthyroidism on procoagulant, anticoagulant and fibrinolytic factors: a systematic review and meta-analysis. Thromb Haemost 2012; 108: 1077-88. 4. Ma C, Zhang Y, Xu Q, Yang J, Zhang Y, Gao L, Xu B, Wang H, Li Y, Lu C, et al. Influence of warfarin dose-associated genotypes on the risk of hemorrhagic complications in Chinese patients on warfarin. Int J Hematol 2012; 96: 719-28. 5. Squizzato A, Romualdi E, Büller HR, Gerdes VE. Clinical review: thyroid dysfunction and effects on coagulation and fibrinolysis: a systematic review. J Clin Endocrinol Metab 2007; 92: 2415-20. 6. Kurnik D, Loebstein R, Farfel Z, Ezra D, Halkin H, Olchovsky D. Complex drug-drug-disease interactions between amiodarone, warfarin, and the thyroid gland. Medicine (Baltimore) 2004; 83: 107-13. 7. Self T, Weisburst M, Wooten E, Straughn A, Oliver J. Warfarin-induced hypoprothrombinemia. Potentiation by hyperthyroidism. JAMA 1975; 231: 1165-6. 8. Vagenakis AG, Cote R, Miller ME, Braverman LE, Stohlman F Jr. Enhancement of warfarin-induced hypoprothrombinemia by thyrotoxicosis. Johns Hopkins Med J 1972; 131: 69-73.
Ji Eun Lee http://orcid.org/0000-0002-8660-0861 Duck Hyun Ryu http://orcid.org/0000-0003-1426-8318 Ho Jung Jeong http://orcid.org/0000-0003-2944-2294 Jung Hoon Kim http://orcid.org/0000-0003-3140-1328 Ji Eun Jun http://orcid.org/0000-0002-7204-4913 June Soo Kim http://orcid.org/0000-0001-7569-6450 Soo Youn Lee http://orcid.org/0000-0002-0662-7408
9. Olchovsky D, Pines A, Zwas ST, Itzchak Y, Halkin H. Apathetic thyrotoxicosis due to hemorrhage into a hyperfunctioning thyroid nodule after excessive anticoagulation. South Med J 1985; 78: 609-11. 10. Tomisti L, Del Re M, Bartalena L, Tanda ML, Pucci A, Pambianco F, Da nesi R, Braverman LE, Martino E, Bogazzi F. Effects of amiodarone, thyroid hormones and CYP2C9 and VKORC1 polymorphisms on warfarin metabolism: a review of the literature. Endocr Pract 2013; 19: 1043-9. 11. Kellett HA, Sawers JS, Boulton FE, Cholerton S, Park BK, Toft AD. Problems of anticoagulation with warfarin in hyperthyroidism. Q J Med 1986; 58: 43-51.
http://dx.doi.org/10.3346/jkms.2014.29.9.1317
http://jkms.org 1319
